Trial management

Trial management


Trial management can encompass entire projects, from strategic design advice to clinical report production, or specific individual tasks.

CERC provides exhaustive services and expert assistance in the whole cycle of clinical trials and clinical data management.

CERC has comprehensive expertise in the design of trials, selection of investigators and sites, creation of study documents, clinical monitoring, core laboratory analysis, data management and compliance with regulatory and quality requirements.

CERC manages a wide variety of clinical trials for both its local and international partners.

The diversity of its team with 18 different languages spoken allows CERC to manage a multi-national trial or a regional one. CERC has the expertise and resources for virtually all of your clinical trial requirements.

CERC has a longstanding successful history of patient enrolment in trials from post market registry to double blind randomized trial. As a clinical research organization, we always endeavour to exceed our sponsors’ expectations.

Follow us